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B Perry

Showing results (921-930 of 1,042) with videos related to

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Human Molecular Genetics|November 8, 2014
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypesAndrew R Wood, Marcus A Tuke, Mike Nalls, et al.
Science Advances|September 14, 2020
The NEMP family supports metazoan fertility and nuclear envelope stiffnessYonit Tsatskis, Robyn Rosenfeld, Joel D Pearson, et al.
Nature Communications|September 30, 2015
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndromeFelix R Day, David A Hinds, Joyce Y Tung, et al.
The New England Journal of Medicine|February 8, 2008
Phenotype and course of Hutchinson-Gilford progeria syndromeMelissa A Merideth, Leslie B Gordon, Sarah Clauss, et al.
Nature|September 15, 2015
The UK10K project identifies rare variants in health and disease, Klaudia Walter, Josine L Min, et al.
European Journal of Endocrinology|April 7, 2025
Deleterious variants in intolerant genes reveal new candidates for self-limited delayed pubertyRaíssa C Rezende, Wen He, Lena R Kaisinger, et al.
Science (New York, N.Y.)|April 28, 2007
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetesEleftheria Zeggini, Michael N Weedon, Cecilia M Lindgren, et al.
Nature Genetics|April 23, 2021
Genetic analyses identify widespread sex-differential participation biasNicola Pirastu, Mattia Cordioli, Priyanka Nandakumar, et al.
Plos Medicine|November 30, 2016
Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation AnalysisLuca A Lotta, Robert A Scott, Stephen J Sharp, et al.
Diabetes|September 12, 2019
Epigenome-Wide Association Study of Incident Type 2 Diabetes in a British Population: EPIC-Norfolk StudyAlexia Cardona, Felix R Day, John R B Perry, et al.
Pageof 105

Showing results (921-930 of 1,042) with videos related to

Sort By:
Pageof 105
Human Molecular Genetics|November 8, 2014
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypesAndrew R Wood, Marcus A Tuke, Mike Nalls, et al.
Science Advances|September 14, 2020
The NEMP family supports metazoan fertility and nuclear envelope stiffnessYonit Tsatskis, Robyn Rosenfeld, Joel D Pearson, et al.
Nature Communications|September 30, 2015
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndromeFelix R Day, David A Hinds, Joyce Y Tung, et al.
The New England Journal of Medicine|February 8, 2008
Phenotype and course of Hutchinson-Gilford progeria syndromeMelissa A Merideth, Leslie B Gordon, Sarah Clauss, et al.
Nature|September 15, 2015
The UK10K project identifies rare variants in health and disease, Klaudia Walter, Josine L Min, et al.
European Journal of Endocrinology|April 7, 2025
Deleterious variants in intolerant genes reveal new candidates for self-limited delayed pubertyRaíssa C Rezende, Wen He, Lena R Kaisinger, et al.
Science (New York, N.Y.)|April 28, 2007
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetesEleftheria Zeggini, Michael N Weedon, Cecilia M Lindgren, et al.
Nature Genetics|April 23, 2021
Genetic analyses identify widespread sex-differential participation biasNicola Pirastu, Mattia Cordioli, Priyanka Nandakumar, et al.
Plos Medicine|November 30, 2016
Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation AnalysisLuca A Lotta, Robert A Scott, Stephen J Sharp, et al.
Diabetes|September 12, 2019
Epigenome-Wide Association Study of Incident Type 2 Diabetes in a British Population: EPIC-Norfolk StudyAlexia Cardona, Felix R Day, John R B Perry, et al.
Pageof 105